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人类肺移植后的免疫抑制治疗。

Immunosuppressive therapy after human lung transplantation.

作者信息

Knoop C, Haverich A, Fischer S

机构信息

Dept of Chest Medicine, Erasme Hospital, Brussels, Belgium.

出版信息

Eur Respir J. 2004 Jan;23(1):159-71. doi: 10.1183/09031936.03.00039203.

Abstract

In 2002, equal numbers of lung transplantation (LTx) were performed with or without induction therapy with antilymphocyte antibodies, monoclonal anti-CD3 antibody or anti-interleukin-2-receptor monoclonal antibodies. It remains to be established if induction therapy after LTx is beneficial or deleterious for long-term graft and patient survival. The vast majority of lung transplant recipients receive a triple-drug maintenance regimen including a calcineurin inhibitor, a cell-cycle inhibitor and steroids. Equal proportions receive cyclosporin A (CsA) and tacrolimus (Tac). There is also a trend to prescribe mycophenolate mofetil (MMF) instead of azathioprine (Aza). Steroid withdrawal is uncommon even 5 yrs after transplantation. The superiority of Tac over CsA as a maintenance agent has not been established to date, and the administration of MMF instead of Aza in combination with CsA and steroids did not improve graft or patient survival in a recent international, prospective, randomised, controlled trial. Shift from cyclosporin A to tacrolimus has emerged as the first treatment step of refractory acute rejection followed by high-dose steroids or antilymphocyte agents, total lymphoid irradiation or photopheresis. The treatment of chronic rejection remains deceptive and includes varied strategies such as modification of the maintenance regimen, addition of inhaled immunosuppressants and/or total lymphoid irradiation and photopheresis.

摘要

2002年,接受肺移植(LTx)的患者中,使用抗淋巴细胞抗体、单克隆抗CD3抗体或抗白细胞介素-2受体单克隆抗体进行诱导治疗与未进行诱导治疗的人数相等。肺移植后诱导治疗对长期移植物和患者生存是有益还是有害,仍有待确定。绝大多数肺移植受者接受包括钙调神经磷酸酶抑制剂、细胞周期抑制剂和类固醇的三联药物维持治疗方案。接受环孢素A(CsA)和他克莫司(Tac)的比例相同。也有一种趋势是开霉酚酸酯(MMF)而不是硫唑嘌呤(Aza)。即使在移植5年后,停用类固醇也不常见。迄今为止,他克莫司作为维持药物优于环孢素A的优势尚未确立,并且在最近一项国际前瞻性随机对照试验中,用霉酚酸酯代替硫唑嘌呤与环孢素A和类固醇联合使用,并未改善移植物或患者的生存率。从环孢素A转换为他克莫司已成为难治性急性排斥反应的首要治疗步骤,随后是大剂量类固醇或抗淋巴细胞药物、全身淋巴照射或光分离置换法。慢性排斥反应的治疗仍然具有欺骗性,包括多种策略,如调整维持治疗方案、添加吸入性免疫抑制剂和/或全身淋巴照射及光分离置换法。

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